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dc.rights.licenseopenen_US
hal.structure.identifierImmunology from Concept and Experiments to Translation = Immunologie Conceptuelle, Expérimentale et Translationnelle [ImmunoConcept]
dc.contributor.authorCOUZI, Lionel
dc.contributor.authorMALVEZZI, P.
dc.contributor.authorAMROUCHE, L.
dc.contributor.authorANGLICHEAU, D.
dc.contributor.authorBLANCHO, G.
dc.contributor.authorCAILLARD, S.
dc.contributor.authorFREIST, M.
dc.contributor.authorGUIDICELLI, G.L.
dc.contributor.authorKAMAR, N.
dc.contributor.authorLEFAUCHEUR, C.
dc.contributor.authorMARIAT, C.
dc.contributor.authorKOENIG, A.
dc.contributor.authorNOBLE, J.
dc.contributor.authorTHAUNAT, O.
dc.contributor.authorTHIERRY, A.
dc.contributor.authorTAUPIN, J.-L.
dc.contributor.authorBERTRAND, D.
dc.date.accessioned2024-09-25T10:36:17Z
dc.date.available2024-09-25T10:36:17Z
dc.date.issued2023
dc.identifier.issn0934-0874en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/201799
dc.description.abstractEnImlifidase recently received early access authorization for highly sensitized adult kidney transplant candidates with a positive crossmatch against an ABO-compatible deceased donor. These French consensus guidelines have been generated by an expert working group, in order to homogenize patient selection, associated treatments and follow-up. This initiative is part of an international effort to analyze properly the benefits and tolerance of this new costly treatment in real-life. Eligible patients must meet the following screening criteria: cPRA ≥ 98%, ≤ 65-year of age, ≥ 3 years on the waiting list, and a low risk of biopsy-related complications. The final decision to use Imlifidase will be based on the two following criteria. First, the results of a virtual crossmatch on recent serum, which shall show a MFI for the immunodominant donor-specific antibodies (DSA) > 6,000 but the value of which does not exceed 5,000 after 1:10 dilution. Second, the post-Imlifidase complement-dependent cytotoxicity crossmatch must be negative. Patients treated with Imlifidase will receive an immunosuppressive regimen based on steroids, rATG, high dose IVIg, rituximab, tacrolimus and mycophenolic acid. Frequent post-transplant testing for DSA and systematic surveillance kidney biopsies are highly recommended to monitor post-transplant DSA rebound and subclinical rejection.
dc.language.isoENen_US
dc.rightsAttribution 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/us/*
dc.subject.enKidney transplantation
dc.subject.enDesensitization
dc.subject.enImlifidase
dc.subject.enHighly sensitized patients
dc.subject.enPositive crossmatch
dc.title.enImlifidase for Kidney Transplantation of Highly Sensitized Patients With a Positive Crossmatch: The French Consensus Guidelines
dc.typeArticle de revueen_US
dc.identifier.doi10.3389/ti.2023.11244en_US
dc.subject.halSciences du Vivant [q-bio]/Immunologieen_US
dc.identifier.pubmed37448448en_US
bordeaux.journalTransplant Internationalen_US
bordeaux.volume36en_US
bordeaux.hal.laboratoriesImmunoConcEpT - UMR 5164en_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.institutionCNRSen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
hal.identifierhal-04709070
hal.version1
hal.date.transferred2024-09-25T10:36:20Z
hal.popularnonen_US
hal.audienceInternationaleen_US
hal.exporttrue
dc.rights.ccCC BYen_US
bordeaux.COinSctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Transplant%20International&rft.date=2023&rft.volume=36&rft.eissn=0934-0874&rft.issn=0934-0874&rft.au=COUZI,%20Lionel&MALVEZZI,%20P.&AMROUCHE,%20L.&ANGLICHEAU,%20D.&BLANCHO,%20G.&rft.genre=article


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